FDA 510(k) Applications Submitted by Eti Zinger

FDA 510(k) Number Submission Date Device Name Applicant
K151654 06/18/2015 PROW FUSION NLT SPINE LTD
K153665 12/21/2015 PROW FUSION-L NLT SPINE LTD
K153786 12/31/2015 PROW FUSION-V NLT SPINE LTD


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